추천 제품
생물학적 소스
synthetic
Quality Level
Grade
ACS reagent
vapor density
1.52 (vs air)
vapor pressure
14.63 psi ( 20 °C)
분석
≥99.5%
형태
liquid
autoignition temp.
365 °F
expl. lim.
60 %
불순물
≤0.008 meq/g Titr. acid
증발 잔류물
≤0.005%
refractive index
n20/D 1.332 (lit.)
bp
21 °C (lit.)
mp
−125 °C (lit.)
solubility
alcohols: soluble
water: miscible
density
0.785 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
CC=O
InChI
1S/C2H4O/c1-2-3/h2H,1H3
InChI key
IKHGUXGNUITLKF-UHFFFAOYSA-N
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일반 설명
Acetaldehyde is an industrially important solvent used as an intermediate for the synthesis of a wide range of compounds. On oxidation it forms acetic acid and ethanol on reduction. The interaction of Criegee intermediate (CH2OO) with acetaldehyde has been measured. Its effect as a neuroactive agent has been studied. Alkynylation reaction of acetaldehyde by asymmetric catalysis has been reported.
애플리케이션
Acetaldehyde may be used in the synthesis of 1,3-diamines by one-pot cross double-Mannich reaction and β-amino aldehydes by proline-catalyzed Mannich reaction.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Carc. 1B - Eye Irrit. 2 - Flam. Liq. 1 - Muta. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-38.0 °F - closed cup
Flash Point (°C)
-38.89 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves
Choose from one of the most recent versions:
이미 열람한 고객
Direct measurement of Criegee intermediate (CH2OO) reactions with acetone, acetaldehyde, and hexafluoroacetone.
Physical Chemistry Chemical Physics, 14(30), 10391-10400 (2012)
Proline-catalysed Mannich reactions of acetaldehyde.
Nature, 452(7186), 453-455 (2008)
Concise Encyclopedia Chemistry, 4-4 (1994)
One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide.
Chemical Communications (Cambridge, England), 49(11), 1118-1120 (2013)
Asymmetric Catalytic Alkynylation of Acetaldehyde: Application to the Synthesis of (+)-Tetrahydropyrenophorol.
Angewandte Chemie (International Edition in English), 51(27), 6704-6708 (2012)
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